DL-acetyltryptophan
group of stereoisomers
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DL-acetyltryptophan
Summary
DL-acetyltryptophan is a group of isomeric entities[1].
Key Facts
- DL-acetyltryptophan's instance of is recorded as group of isomeric entities[2].
- DL-acetyltryptophan's CAS Registry Number is recorded as 87-32-1[3].
- DL-acetyltryptophan's EC number is recorded as 201-739-3[4].
- DL-acetyltryptophan's canonical SMILES is recorded as CC(=O)NC(CC1=CNC2=CC=CC=C21)C(=O)O[5].
- DL-acetyltryptophan's InChI is recorded as InChI=1S/C13H14N2O3/c1-8(16)15-12(13(17)18)6-9-7-14-11-5-3-2-4-10(9)11/h2-5,7,12,14H,6H2,1H3,(H,15,16)(H,17,18)[6].
- DL-acetyltryptophan's InChIKey is recorded as DZTHIGRZJZPRDV-UHFFFAOYSA-N[7].
- DL-acetyltryptophan's chemical formula is recorded as C₁₃H₁₄N₂O₃[8].
- DL-acetyltryptophan's subclass of is recorded as tryptamine alkaloid[9].
- DL-acetyltryptophan's MeSH descriptor ID is recorded as C006392[10].
- DL-acetyltryptophan's ChEMBL ID is recorded as CHEMBL1905494[11].
- DL-acetyltryptophan's UNII is recorded as 4460NBV53F[12].
- DL-acetyltryptophan's ChemSpider ID is recorded as 1925[13].
- DL-acetyltryptophan's PubChem CID is recorded as 2002[14].
- DL-acetyltryptophan's ChEBI ID is recorded as 70976[15].
- DL-acetyltryptophan's found in taxon is recorded as Aspergillus nidulans[16].
- DL-acetyltryptophan's found in taxon is recorded as Penicillium commune[17].
- DL-acetyltryptophan's found in taxon is recorded as soybean[18].
- DL-acetyltryptophan's found in taxon is recorded as Bacillus pumilus[19].
- DL-acetyltryptophan's Reaxys registry number is recorded as 487262[20].
- DL-acetyltryptophan's Human Metabolome Database ID is recorded as HMDB0255052[21].
- DL-acetyltryptophan's KNApSAcK ID is recorded as C00059444[22].
- DL-acetyltryptophan's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+246.1'}[23].
- DL-acetyltryptophan's ECHA Substance Infocard ID is recorded as 100.001.582[24].
- DL-acetyltryptophan's NSC number is recorded as 49124[25].
- DL-acetyltryptophan's subject has role is recorded as protease inhibitor[26].